Search results

Showing 1 – 9 of 9 results.

Curated

Established Populations for Epidemiologic Studies of the Elderly, 1981-1993: [East Boston, Massachusetts, Iowa and Washington Counties, Iowa, New Haven, Connecticut, and North Central North Carolina] (ICPSR 9915)

Released/updated on: 2006-01-18

Geographic coverage: North Carolina, Iowa, New Haven, United States, Massachusetts, Connecticut, Boston

Time period: 1981-01-01--1993-12-31

The goals of the Established Populations for Epidemiologic Studies of the Elderly (EPESE) project were to describe and identify predictors of mortality, hospitalization, and placement in long-term care facilities and to investigate risk factors for chronic diseases and loss of functioning. The survey elicited information from persons 65 years of age and older in four geographic locations: East Boston, Massachusetts, New Haven, Connecticut, Iowa and Washington Counties, Iowa, and five counties in north central North Carolina. The public use baseline data (Part 1) cover demographic characteristics (age, sex, race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Data from six follow-up surveys conducted in all four of the sites are also provided (Parts 2-4 and 6-8), along with information from death certificates for deaths occurring in the first six years of follow-up for all four sites (Part 5).

Curated

Hispanic Health and Nutrition Examination Survey, 1982-1984 (ICPSR 8535)

Released/updated on: 2006-01-12

Geographic coverage: United States

Time period: 1982-07-01--1984-12-31

Sixteen components focusing on nutritional practices and physical health comprise this survey of Hispanic Americans. The Body Measurements file includes anthropometric data on individuals such as skeletal and skin fold measurements, body circumferences, height, and weight. The Dental Health data provide dental history information, including the frequency of and reasons for visits to a dental hygienist, fluoride treatments, and the results of a clinical examination. The Blood and Urine Assessments component of the study contains clinical data such as red and white blood cell counts, serum iron and vitamin levels, amount of lead, and other assays. The Physician's Examination file provides the results of a basic physical exam, and the Dietary Practices/Food Frequency component includes information on food recall, special diets, frequency of meals, and consumption of various types of foods. The Adolescent and Adult History Questionnaire file supplies information on health care and problems getting care, dental care, health status, conditions, medical treatment, pesticide exposure, smoking, acculturation, meal programs for school-age children, reproductive history, and health status of children. Measures of Depression provides data on feelings of depression, how depression affected everyday life, help sought during depression, and weight changes and sleep loss due to depression. The Alcohol Consumption Data section includes information on the amount and kind of alcohol consumed, reasons for drinking, and self-perception of drinking habits. The Drug Abuse file offers information on the use of barbiturates and other sedatives, marijuana and hash, inhalants, and cocaine. The Hearing data were collected during the physical examination and provide information on respondents' ability to hear and the condition of their hearing organs. The Gallbladder Ultrasound data include information on disease, history of symptoms, findings of ultrasounds, and physical examinations of the gallbladder. Diabetes and OGTT (oral glucose tolerance test) data were also collected. Respondents were asked whether they had diabetes and were also questioned about age of onset, medication taken, diet, and if the OGTT had been administered. The file also contains detailed information on the OGTT, diet before the testing, time intervals between blood drawings, and plasma glucose values in milligrams and deciliters. The Vision section furnishes information on the respondent's eyesight, whether he or she had a problem seeing, appliances worn, age when corrective lenses were first worn, if a doctor had been visited for sight problems, and findings from a physician's examination. Measurements of the respondent's visual acuity with and without correction are also included in the data. The Child History section includes information on health status, health care utilization, infant feeding practices, participation in meal programs, school attendance, and language use. The 24-Hour Recall lists amounts of calories, protein, total fat, fatty acids, cholesterol, carbohydrates, dietary fiber, alcohol, vitamins, and minerals for each food item consumed by each person. It also contains a description of the food, ingestion period, approximate time of consumption, and food source. The data from the Measurement and Interpretation of Electrocardiograms file give an objective measure of the cardiac health status of individuals examined in the survey. Despite the limitations of such data, the electrocardiographic variables are carefully and completely defined. Also, an extensive process was used to ensure the accuracy of the findings. In addition, each part of this collection provides sociodemographic data, such as age, race, national origin, birthplace, education, employment, insurance, and use of public assistance. Also included are family data including number of people in the family, family income, poverty index, use of food stamps, and size of residence.

Curated

National Health and Nutrition Examination Survey I: Epidemiologic Follow-Up Study, 1982-1984 (ICPSR 8900)

Released/updated on: 2006-01-18

Geographic coverage: United States

Time period: 1982-01-01--1984-12-31

The National Health and Nutrition Examination Survey I Epidemiologic Followup Study (NHEFS) originated as a joint project between the National Center for Health Statistics (NCHS) and the National Institute on Aging (NIA). The design of NHEFS, which contains follow-up data on the NHANES I cohort, consisted of five steps. The first step focused on tracing and locating all subjects in the cohort or their proxies and determining their vital status. The second step involved the obtaining of death certificates for subjects who were deceased. Interviews with the participants or their proxies constituted the third phase of the follow-up. The fourth phase of the follow-up included measurements of pulse, blood pressure, and weight for interviewed respondents, and the fifth step was the acquisition of relevant hospital and nursing home records, including pathology reports and electrocardiograms. The respondent interview was designed to gather information on selected aspects of the subject's health history since the time of the NHANES I exam. This information included a history of the occurrence or recurrence of selected medical conditions, an assessment of behavioral, social, nutritional, and medical risk factors believed to be associated with these conditions, and an assessment of various aspects of functional status. Whenever possible, the questionnaire was designed to retain item comparability between NHANES I and NHEFS in order to measure change over time. However, questionnaire items were modified, added, or deleted when necessary to take advantage of recent improvements in questionnaire methodology. The Vital and Tracing Status file is a master file containing tracing, vital status, and demographic data for all NHEFS respondents. In addition, it provides users with information on the availability of different survey components for each respondent. For example, variables have been created to indicate whether a death certificate was received for a deceased subject, hospital records were received, or a follow-up interview was completed. The Health Care Facility Record file offers data on respondents who had reported an overnight stay in a health care facility after 1970. Information on the name and address of the facility, the date of the stay, and the reason for the stay was recorded. The Mortality Data file contains death certificate information for 1,935 NHEFS decedents. The death certificate information is for deaths occurring from 1971 to 1983.

Curated

National Health and Nutrition Examination Survey II, 1976-1980: Medical History Ages 12-74 Years (ICPSR 8183)

Released/updated on: 1992-02-16

Geographic coverage: United States

Time period: 1976-01-01--1980-12-31

The Health and Nutrition Examination Survey II, 1976-1980: Medical History ages 12-74 years contains demographic characteristics and health histories of 18,447 interviewed persons 12-74 years of age. The medical histories include items on medication, hospital care, tuberculosis, a variety of acute and chronic diseases, tobacco usage, physical activity, weight, height, vision disability, exposure to pesticides, gastrointestinal problems, and, for females, a menstrual and pregnancy history. Data were also collected on anemia, diabetes, respiratory conditions, hearing and speech, liver and gallbladder conditions, kidney and bladder disease, allergies, hypertension, cardiovascular conditions, stroke, arthritis (stressing middle and upper back and neck problems), and participation in food programs.

Curated

National Mortality Followback Survey, 1993 (ICPSR 2900)

Released/updated on: 2005-02-21

Geographic coverage: United States

Time period: 1993-01-01--1993-12-31

The National Mortality Followback Survey (NMFS) Program, begun in the 1960s by the National Center for Health Statistics (NCHS), uses a sample of United States residents who die in a given year, supplementing information derived from the death certificate with information from the next of kin or another person familiar with the decedent's life history. This information, sometimes enhanced by administrative records, is collected in order to study the etiology of disease, demographic trends in mortality, and other health issues. The 1993 National Mortality Followback Survey (NMFS) sampled individuals aged 15 years and over who died in 1993. Forty-nine of the 50 state vital registration areas, as well as the independent vital registration areas of the District of Columbia and New York City, granted approval to sample their death certificates. (South Dakota declined to participate due to a state law restricting the use of death certificate information.) A sample of 22,957 death certificates from 1993 was then drawn. To obtain reliable numbers for important population subgroups, such as persons under age 35, women, and the Black population, death certificates from those subgroups were oversampled. The 1993 NMFS survey focused on five subject areas: (1) socioeconomic differentials in mortality, (2) associations between risk factors and cause of death (use of tobacco, alcohol, drugs, firearms, motor vehicles), (3) disability (medical condition and cognitive functioning during the last year of life), (4) access and utilization of health care facilities during the last year of life (number of doctor visits, days bedridden, nursing home experiences, use of assistive medical devices, availability of health insurance), and (5) reliability of certain items reported on the death certificate. Demographic variables include age, gender, race, marital status, birthplace, education, occupation and industry, and income and assets. The 1993 NMFS survey differed from the previous mortality followback surveys in several ways: First, it emphasized deaths due to homicide, suicide, and unintentional injury. Second, the subject areas were considerably broader (many previously-surveyed subject areas, however, are included for trend analysis). This survey was also the first to acquire national-level information from medical examiners and coroners. Finally, the complexity of the questionnaire necessitated telephone or in-person interviews. The 1993 NMFS was designed in collaboration with other agencies of the Public Health Service, Department of Health and Human Services, and the National Highway Traffic Safety Administration.

Curated

National Survey of the Aged [United States], 1957 (ICPSR 7686)

Released/updated on: 2006-03-30

Geographic coverage: United States

Time period: 1957-01-01--1957-12-31

This survey, sponsored by the Health Information Foundation at the University of Chicago and conducted at the National Opinion Research Center, consists of three component parts. Part 1, the Health Needs of Older Persons, covers health, the use of medical facilities, the cost of medical care, the older person's sources of income, his/her social relationships, attitudes toward younger family members, work, religion, and a self-evaluation of health status for persons aged 60 and over. Part 2, Household Enumeration: Noninterviewed Individuals, contains information describing persons located during the enumeration process who were unable to complete an interview. For Part 3, Public Attitudes on Older People, a cross-section of adult Americans was surveyed. This survey was mainly concerned with the level of responsibility younger and middle-aged people assumed for older relatives, the kinds of plans they were making for their own maintenance in later years, and overall attitudes on the part of all age groups toward certain situations that are commmon in later life.

Curated

Partially restricted

Simple Crosstabs

Project Migrante: Health Status and Access to Health Care Among Migrants on Mexico's Northern Border, 2020-2021 (ICPSR 38601)

Released/updated on: 2023-06-07

Geographic coverage: Tijuana, Matamoros, Mexico, Ciudad Juárez

Time period: 2020-01-01--2021-12-31

The Migrante Project is a binational study that examines health status and access to health care among Mexican migrants. Since 2007, Migrante investigators have implemented a series of cross-sectional probability-based surveys on Mexico's northern border. The current phase of Migrante includes three survey waves (N=1,200 each), each focused on a specific topic area. Data for the Wave I survey focused on HIV and sexual/reproductive health. Wave II is focused on non-communicable disease. Data collection for this wave is ongoing. Wave III (data to be collected in 2023) will focus on mental health and substance use. All surveys contain additional questions on socio-demographics, health status, health care access, migration history, and contextual factors related to migration stage. All waves also include biometric testing (for example, rapid HIV testing). Participants are sampled from four different migrant flows:

Northbound flow: Migrants traveling north and arriving at the border from other regions in Mexico
Southbound flow - Border: Migrants traveling from the Mexico side of the Mexico-US border to points farther south
Southbound flow - U.S.: Migrants returning to Mexico from the U.S. voluntarily
Deported flow: Migrants returning to Mexico from the U.S via deportation

The data herein come from the Wave I survey and were collected in Tijuana, Matamoros, and Ciudad Juárez, Mexico between August 2020 and September 2021. The study employed a multistage sampling design, with a combination of geographic and temporal sampling units, modeled after the Encuesta sobre Migración en la Frontera Norte de México (EMIF Norte). Migrante sampling sites for Wave I included bus stations, airports, and deportation stations in each of the three cities.

Eligible individuals were at least 18 years old, born in Mexico or other Latin American countries, fluent in Spanish, not residents of the city where the survey is being conducted (except for deported migrants), and traveling for labor reasons or change of residence. In total, there were 1,398 observations (northbound flow N=347, southbound flow N=703, and deported flow N=348) in Wave I, with 1,257 individuals completing the Wave I survey. Three hundred and six of these individuals belonged to the deported flow, 306 to the northbound flow, 336 to the southbound border flow, and 309 to the southbound U.S. flow. Consent rates ranged from 13% to 98% depending on the flow and survey city. Migrante surveys can be used to produce population-level estimates of health outcomes and health care access, investigate variations across migration phases, and explore the impact of health care and immigration policies on migrants' health outcomes, healthcare access, and individual and environmental health determinants.

Curated

Restricted

Social Environment and Biomarkers of Aging Study (SEBAS) in Taiwan, 2000 and 2006 (ICPSR 3792)

Released/updated on: 2014-06-17

Geographic coverage: Taiwan

Time period: 2000-01-01--2000-12-31, 2006-01-01--2006-12-31

The Social Environment and Biomarkers of Aging Study (SEBAS) in Taiwan, 2000 and 2006, provides information regarding the health and well-being of older persons in Taiwan. Taiwan has undergone rapid demographic, social, and economic changes, becoming a highly urbanized and industrial society with a growing population of persons age 65 or older. SEBAS explores the relationship between life challenges and mental and physical health, the impact of social environment on the health and well-being of the elderly, as well as biological markers of health and stress. The study collected self-reports of physical, psychological, and social well-being, plus extensive clinical data based on medical examinations and laboratory analyses. Examination of health outcomes included chronic illnesses, functional status, psychological well-being, and cognitive function. Questions regarding life challenges focused on perceived stress, economic difficulties, security and safety, and the consequences of a major earthquake. Biological markers were used to identify cardiovascular risk factors, metabolic process measures, immune-system activity, the hypothalamic-pituitary adrenal axis, and sympathetic nervous system activity. Two rounds of biomarker data collected in 2000 and 2006 were complemented by face-to-face interviews with the participants. Demographic and background variables included age, sex, education, ethnicity, occupation, and residency.

Additional information about the Social Environment and Biomarkers of Aging Study can be found at the Georgetown University Center for Populations and Health Web site.

A Webinar describing the Social Environment and Biomarkers of Aging Study (SEBAS) was presented June 20, 2016. All interested users can access the webinar here.

Curated

Tecumseh Community Health Study, 1959-1969 (ICPSR 8969)

Released/updated on: 1992-02-16

Geographic coverage: United States, Tecumseh, Michigan

The Tecumseh Community Health Study is a longitudinal, ongoing prospective epidemiologic study of a natural community's health and disease status. Data have been collected on the Tecumseh population in southeast Michigan for over 30 years, beginning with a 1957 canvass of all households and adding all newcomers to the community until 1970, after which only previous residents have been followed. The Tecumseh project has conducted over 80 different studies, including both disease-specific investigations and studies concerned with the prevalence and incidence of disease in the community. The core data file for the years 1959-1969 contains data collected in Round I: 1959-1960, Round II: 1962-1965, and Round III: 1967-1969 (referred to as the Cardiovascular Studies I, II, and III, and the General Surveillance Study II). These data include information taken from baseline medical history interviews, medical examinations, clinical measurements, laboratory work, and electrocardiograms. Mortality status of all persons at the time of attempted or actual contact in Round III is also provided. The major variable groups include demographic information, family history of major diseases, systematic review of present and past symptoms and conditions, smoking and drinking habits, physical examinations, measurements and laboratory work, and electrocardiogram results.